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Research Associate Downstream Process Development Jobs in Brookhaven, MS

ICON

Clinical Research Coordinator

Mccomb, MS · On-site

$21 - $27.75/hr

Learning and development opportunities through structured training and career pathways Benefits may ... If you require reasonable accommodations during the recruitment process, please let us know or ...

LC Industries

Technician, QA

Hazlehurst, MS · On-site

To that end, we engage in philanthropic efforts for research into blindness and treatment for the visually impaired. ABOUT THIS ROLE The Technician, QA performs process development. Analysis ...

L C Industries

Technician, QA

Hazlehurst, MS · On-site

To that end, we engage in philanthropic efforts for research into blindness and treatment for the visually impaired. ABOUT THIS ROLE The Technician, QA performs process development. Analysis ...

Cableone

Field Technician

Mccomb, MS · On-site

$17 - $23.25/hr

You will ensure we are providingproper upstream and downstream signal levels at each termination on ... Pre-hire Processes Cable One and our family of brands is committed to keeping our associates and ...

TJX Companies

ARRC Assoc

Hazlehurst, MS · On-site

$15.15 - $18.95/hr

... and prioritizes your development. Whether you're working in our four global Home Offices ... Extracting boxes and selection process at the baler for reuse * Unloading fixtures and boxes from ...

Ross Stores

Retail Associate

Mccomb, MS

$13.25 - $15/hr

... development for our teams GENERAL PURPOSE: The Retail Associate is responsible for ensuring our ... Manages Work Processes Business Acumen Plans, Aligns & Prioritizes Builds Talent Collaborates ...

Ross Stores

Retail Associate

Mccomb, MS · On-site

$13.25 - $15/hr

... development for our teams. GENERAL PURPOSE: The Retail Associate is responsible for ensuring our ... Manages Work Processes * Business Acumen * Plans, Aligns & Prioritizes * Builds Talent

Cable One, Inc.

Field Technician

Mccomb, MS · On-site

$17 - $23.25/hr

... and downstream signal levels at each termination on the customer's premises. • You will be ... Pre-hire Processes Cable One and our family of brands is committed to keeping our associates and ...

Cable One

Field Technician

Mccomb, MS · On-site

$17 - $23.25/hr

... and downstream signal levels at each termination on the customer's premises. · You will be ... Pre-hire Processes Cable One and our family of brands is committed to keeping our associates and ...

Tjx

ARRC Assoc

Hazlehurst, MS · On-site

$15.15 - $18.95/hr

... and prioritizes your development. Whether you're working in our four global Home Offices ... Extracting boxes and selection process at the baler for reuse * Unloading fixtures and boxes from ...

TJX Companies

ARRC Assoc

Hazlehurst, MS · On-site

$15.15 - $18.95/hr

... and prioritizes your development. Whether you're working in our four global Home Offices ... Extracting boxes and selection process at the baler for reuse * Unloading fixtures and boxes from ...

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All JobsResearch Associate Downstream Process Development JobsResearch Associate Downstream Process Development Jobs in Brookhaven, MS

Research Associate Downstream Process Development information

See Brookhaven, MS salary details

$14

$26

$38

How much do research associate downstream process development jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for research associate downstream process development in Brookhaven, MS is $26.13, according to ZipRecruiter salary data. Most workers in this role earn between $21.44 and $32.07 per hour, depending on experience, location, and employer.

What is a research associate downstream process development?

A Research Associate in Downstream Process Development works within biotechnology or pharmaceutical companies to optimize and scale up the purification and recovery of biological products, such as proteins or antibodies, after initial production. They focus on processes like filtration, chromatography, and centrifugation to ensure product quality and yield. These professionals design experiments, analyze data, and support the transfer of processes from laboratory scale to manufacturing. Their work is crucial for developing efficient, reproducible, and regulatory-compliant methods for producing biopharmaceuticals.

What are the key skills and qualifications needed to thrive as a research associate in downstream process development?

To thrive as a Research Associate in Downstream Process Development, you need a solid background in biochemistry, molecular biology, or chemical engineering, often demonstrated by a bachelor's or master's degree in a related field. Familiarity with chromatography systems (such as AKTA), filtration technologies, and Good Manufacturing Practice (GMP) standards, along with data analysis software, is typically required. Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities help individuals excel in this role. These competencies are crucial for ensuring efficient, scalable purification processes and maintaining product quality in biopharmaceutical development.

What are the typical challenges faced by a research associate in downstream process development, and how can they be addressed?

A Research Associate in Downstream Process Development often encounters challenges such as optimizing purification processes for new biologics, troubleshooting equipment issues, and ensuring scalability from laboratory to production scale. Effective communication with cross-functional teams, such as upstream scientists and analytical specialists, is essential to resolve issues quickly. Staying current with new purification technologies and maintaining meticulous documentation can also help address these challenges and support successful process development.

What is the difference between Research Associate Downstream Process Development vs Research Associate Upstream Process Development?

AspectResearch Associate Downstream Process DevelopmentResearch Associate Upstream Process Development
Primary FocusPurification, filtration, chromatography of bioproductsCell culture, media optimization, bioreactor operation
Skills & CertificationsProtein purification, chromatography techniques, GMP complianceCell culture, aseptic techniques, bioreactor handling
Work EnvironmentLaboratory, manufacturing, quality controlLaboratory, bioprocessing facilities
Industry UsageBiopharmaceutical manufacturing, biotech researchBiopharmaceutical development, biotech research

While both roles support bioprocess development, Research Associate Downstream Process Development focuses on purification and filtration of bioproducts, whereas Research Associate Upstream Process Development emphasizes cell culture and bioreactor processes. Understanding these differences helps candidates align their skills with the appropriate role in biopharmaceutical production.

What cities near Brookhaven, MS are hiring for Research Associate Downstream Process Development jobs?

Cities near Brookhaven, MS with the most Research Associate Downstream Process Development job openings:

Research Associate Downstream Process Development jobs near you
Infographic showing various Research Associate Downstream Process Development job openings in Brookhaven, MS as of August 2026, with employment types broken down into 89% Full Time, and 11% Contract. Highlights an 97% In-person, and 3% Remote job distribution, with an average salary of $54,346 per year, or $26.1 per hour.

Clinical Research Coordinator

Mccomb, MS • On-site

ICON
See more jobs at ICONexternal

$21 - $27.75/hr

Part-time

Medical, Dental, Vision, Life, Retirement

Posted 8 days ago

Job description

Clinical Research Coordinator- McComb, MS
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Clinical Research Coordinator at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
Your role will involve delivering clinical coordination work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
  • Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
  • Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure compliance with study protocols, regulatory requirements, and ethical standards.
  • Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes.
  • Managing study-related documentation, including informed consent forms, case report forms, and regulatory submissions.
  • Providing support and guidance to study participants, including education, counseling, and assistance with study-related procedures.

Your Profile:
You will bring relevant clinical coordination experience, along with the following qualifications and skills.
Required qualifications and experience:
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field.
  • Previous experience working in clinical research or healthcare settings preferred.
  • Knowledge of clinical research regulations, including FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
  • Strong organizational, communication, and interpersonal skills, with the ability to work effectively in a team environment.
  • Detail-oriented with the ability to manage multiple tasks and priorities simultaneously.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply

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